Zhuma T, Tyrrell R, Sekkali B, Skavdis G, Saveliev A, Tolaini M, Roderick K, Norton T, Smerdon S, Sedgwick S, Festenstein R, Kioussis D
Division of Molecular Immunology, National Institute for Medical Research, The Ridgeway, Mill Hill, London NW7 1AA, UK.
EMBO J. 1999 Nov 15;18(22):6396-406. doi: 10.1093/emboj/18.22.6396.
The locus control region (LCR) of the human CD2 gene (hCD2) confers T cell-specific, copy-dependent and position-independent gene expression in transgenic mice. This LCR consists of a strong T cell-specific enhancer and an element without enhancer activity (designated HSS3), which is required for prevention of position effect variegation (PEV) in transgenic mice. Here, we identified the HMG box containing protein-1 (HBP1) as a factor binding to HSS3 of the hCD2 LCR. Within the LCR, HBP1 binds to a novel TTCATTCATTCA sequence that is higher in affinity than other recently reported HBP1-binding sites. Mice transgenic for a hCD2 LCR construct carrying a deletion of the HBP1-binding sequences show a propensity for PEV if the transgene integrates in a heterochromatic region of the chromosome such as the centromere or telomere. We propose that HBP1 plays an important role in chromatin opening and remodelling activities by binding to and bending the DNA, thus allowing DNA-protein and/or protein-protein interactions, which increase the probability of establishing an active locus.
人类CD2基因(hCD2)的基因座控制区(LCR)在转基因小鼠中赋予T细胞特异性、拷贝数依赖性和位置独立性的基因表达。该LCR由一个强大的T细胞特异性增强子和一个无增强子活性的元件(命名为HSS3)组成,后者是转基因小鼠中防止位置效应斑驳(PEV)所必需的。在此,我们鉴定出含HMG盒蛋白-1(HBP1)作为与hCD2 LCR的HSS3结合的因子。在LCR内,HBP1与一个新的TTCATTCATTCA序列结合,该序列的亲和力高于其他最近报道的HBP1结合位点。携带HBP1结合序列缺失的hCD2 LCR构建体的转基因小鼠,如果转基因整合到染色体的异染色质区域如着丝粒或端粒,则显示出PEV倾向。我们提出,HBP1通过与DNA结合并使其弯曲,在染色质开放和重塑活动中发挥重要作用,从而允许DNA-蛋白质和/或蛋白质-蛋白质相互作用,这增加了建立活性基因座的可能性。